Clinical Research Coordinator II

•Experienced | Rheumatology Research Confidential Bellevue, WA Job Details Full-time $30

•$35 an hour 1 hour ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Qualifications Teamwork Clinical research Laboratory experience Bachelor's degree Patient care Materials handling Full Job Description Job Overview

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APPLICANTS MUST ALREADY RESIDE IN THE SEATTLE AREA

We are actively seeking a Clinical Research Coordinator (CRC) with 3+ years of clinical research experience to join our dedicated and expanding research team. This is a full-time, on-site position ideal for a skilled coordinator who is passionate about clinical trials and committed to advancing care in rheumatologic diseases. The CRC will work closely with the Clinical Research Manager and Principal/Sub-Investigators to independently manage multiple industry-sponsored drug trials from start to finish. If you're an experienced research professional looking to deepen your expertise in a collaborative environment while making a meaningful impact on patient access to innovative therapies, we encourage you to apply.

APPLICANTS MUST ALREADY RESIDE IN THE SEATTLE AREA

•THIS

IS A FULL TIME IN PERSON ON SITE POSTION.

There is NO relocation opportunity for this position. Please note the salary range for this position is: $30-35/hour

APPLICANTS WHO DO NOT ALREADY LIVE IN THE SEATTLE AREA WILL NOT BE EVALUATED FOR THIS POSTION.

Duties Ensure the study-specific informed consent is signed by the subjects or the caregivers. Code, evaluate, or interpret collected study data. Maintain required records of study activity, including case report forms, drug dispensation records, or regulatory forms. Communicate with laboratories or investigators regarding laboratory findings. Solicit industry-sponsored trials through contacts and professional organizations. Order drugs or devices necessary for study completion. Direct the requisition, collection, labeling, storage, or shipment of specimens. Arrange research study sites and determine staff or equipment availability. Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues. Register protocol patients with appropriate statistical centers as required. Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Perform specific protocol procedures such as taking vital signs and performing electrocardiograms. Prepare lab samples for overnight shipment, including handling of dry ice (prefer IATA certification). Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics. Develop advertising and other informational materials to be used in subject recruitment. Contact industry representatives to ensure the equipment and software specifications necessary for successful study completion. Confer with health care professionals to determine the best recruitment practices for studies. Organize space for study equipment and supplies. Track enrollment status of subjects and document dropout information, such as dropout causes and subject contact efforts. Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks. Record adverse events and side effect data and confer with investigators regarding the reporting of events to oversight agencies. Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports. Oversee subject enrollment to ensure that informed consent is properly obtained and documented. Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data. Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures. Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions. Dispense medical devices or drugs and calculate dosages and provide instructions as necessary. Contact outside health care providers and communicate with subjects to obtain follow-up information. Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions. Schedule subjects for appointments and procedures as required by study protocols, and ensure subject compliance with visit attendance.

Bonus skills:

Thorough knowledge of CRIO and EDC. Experience

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APPLICANTS MUST ALREADY RESIDE IN THE SEATTLE AREA

The ideal candidate will have: Bachelor's degree in a science or healthcare-related field required (Biology preferred). Minimum of 3 years of U.S

•based clinical research coordination experience (industry-sponsored trials preferred). Demonstrated commitment to research as a long-term career path. Excellent interpersonal, organizational, and communication skills. Familiarity with

CRIO, EDC

systems, and sample processing protocols is highly desirable. Must be able to handle dry ice and coordinate biological sample shipments (IATA preferred) COVID-19 and other CDC-recommended vaccinations required prior to start

APPLICANTS MUST ALREADY RESIDE IN THE SEATTLE AREA

Why Join Us? You'll become part of a close-knit, mission-driven team focused on improving care access and outcomes for patients with chronic autoimmune diseases. You'll have the opportunity to contribute meaningfully to trial design and execution, expand your skill set, and be supported in your professional growth within the research field.

APPLICANTS MUST ALREADY RESIDE IN THE SEATTLE AREA

Job Type:

Full-time Pay:

$30.00

•$35.00 per hour

Benefits:

401(k) Dental insurance Health insurance Paid time off Vision insurance Application Question(s): 3 years of U.S

•based clinical research coordination Currently living in the Seattle/Bellevue Area?

Education:

Bachelor's (Required)

Experience:

Clinical research: 3 years (Required) Ability to

Commute:

Bellevue, WA 98004 (Required)

Work Location:

In person